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Detects genetic mutations associated with Prader-Willi and Angelman syndromes.

33,600 THB

A two-step genetic test involving QF-PCR and karyotyping for prenatal diagnosis of chromosomal disorders.

12,075 THB

Screens for carrier status of Spinal Muscular Atrophy and Fragile-X Syndrome.

23,310 THB

Detects chromosomal abnormalities (trisomy 21) associated with Down syndrome.

8,505 THB

Measures organic acids in urine, used to diagnose inborn errors of metabolism.

10,878 THB

Detects genetic mutations through whole exome sequencing, used in diagnosing rare genetic disorders.

78,750 THB

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